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Mendelian traits behave according to the model of monogenic or simple gene inheritance in which one gene corresponds to one trait. Discrete traits (as opposed to continuously varying traits such as height) with simple Mendelian inheritance patterns are relatively rare in nature, and many of the clearest examples in humans cause disorders.
Autosomal dominant A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]
Human genetics is the study of inheritance as it occurs in human beings.Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.
The study of human genetic variation has evolutionary significance and medical applications. It can help scientists reconstruct and understand patterns of past human migration. In medicine, study of human genetic variation may be important because some disease-causing alleles occur more often in certain population groups.
The hominoids are descendants of a common ancestor.. Homo sapiens is a distinct species of the hominid family of primates, which also includes all the great apes. [1] Over their evolutionary history, humans gradually developed traits such as bipedalism, dexterity, and complex language, [2] as well as interbreeding with other hominins (a tribe of the African hominid subfamily), [3] indicating ...
Eye color is an example of a (physical) phenotypic trait. A phenotypic trait, [1] [2] simply trait, or character state [3] [4] is a distinct variant of a phenotypic characteristic of an organism; it may be either inherited or determined environmentally, but typically occurs as a combination of the two. [5]
Monogenic may refer to: Monogenic signal, in the theory of analytic signals; Monogenic disorder, disease, inheritance, or trait, a single gene disorder resulting from a single mutated gene. Monogenic diabetes, or maturity-onset diabetes of the young (MODY), forms of diabetes caused by mutations in an autosomal dominant gene; Monogenic obesity
Monogenism or sometimes monogenesis is the theory of human origins which posits a common descent for all humans. The negation of monogenism is polygenism.This issue was hotly debated in the Western world in the nineteenth century, as the assumptions of scientific racism came under scrutiny both from religious groups and in the light of developments in the life sciences and human science.